• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    There is disclosed a new process for preparing coupled and coextruded multilayer articles (consisting of two or more layers) made of thermoplastic materials, and closed-surface bodies comprising the same. The process comprises (a) feeding, to an extruder connected with a coextrusion head, a polyvinyl alcohol having a high degree of hydrolysis mixed with an aqueous mixture of plasticizing compounds and heated under pressure to bring it to the plastisol state; (b) subjecting the plastisol polyvinyl alcohol to rapid decompression with simultaneous venting of the evolved vapors, before it enters the coextrusion head and while it is at a temperature at least equal to, and preferably higher than, the temperature of the coextrusion head; (c) separately feeding at least one other thermoplastic polymer to the same coextrusion head; (d) adjusting the temperature of the polymers, after contact thereof, so that the temperature of the polyvinyl alcohol is at least equal to, and preferably higher than, the temperature of the other coextruded polymer or polymers; (e) adjusting the flow rate of the polymers so that the outflow linear velocities thereof are equal or differ no more than +/-10%; and (f) molding the coextruded article leaving the coextrusion head into a manufactured article.
    公开号:SU871735A3
    申请号:SU772453393
    申请日:1977-02-17
    公开日:1981-10-07
    发明作者:Раналли Франко；Ортолани Леоне；Тиси Квинто
    申请人:Монтэдисон С.П.А. (Фирма)；Ортолани Леоне；
    IPC主号:
    专利说明:

    one
    The invention relates to the field of processing plastic masSg specifically to products with a closed surface made of laminates and to a method for their manufacture.
    Laminated articles are known / possessing reduced princi- palability and consisting of thermoplastic layers / for example from layers of homopolymers or co-V polymers of vinyl chloride and vinylidene chloride l.
    The product is prepared by a method / involving the co-extrusion of various thermoplastics 21 - The disadvantage of this method is that thermoplastic polymers, which are capable of hot-pressing and hot-pressing, have a high permeability to gas and water 20 pagras. than they cannot be used for packaging foodstuffs, medical products, for the production of beshlon for soda water or internal chambers, for 25 pressured two-section vessels, and so on.
    Vinylidene copolymers have a high impermeability, but their use is limited by the complexity of the AO-ZO.
    work in the manufacture of fine products, as well as low tensile and hot welding, low modulus of elasticity, low resistance and so on.
    Other polymers, such as polyvinyl alcohol, with a relatively high degree of hydrolysis have a high impermeability to gases, vapors and odors, but are sensitive to water and are poorly mechanically treated.
    When molding products made from polyvinyl alcohols, pressed at temperatures above 100 ° C by conventional methods, more or less intense formation of vapor bubbles occurs due to the rapid evaporation of water used as a plasticizer for the polymer.
    In addition, a disadvantage of vinyl alcohol-based polymers is that in many wet conditions their oxygen tightness is not high.
    The aim of the invention is to improve the gas tightness.
    This goal is achieved by obtaining a layered product consisting of two or three alternating layers made of thermoplastic materials, one layer made of polyvinyl alcohol with a polymerization degree of 1000-1100 and a degree of hydrolysis of 88-89 mol.%, And another layer It is made of a thermoplastic polymer selected from the group consisting of polyethylene, polyvinyl chloride, polyethylene, J-terephthalate and nylon. Such a product is made by coextrusion of two or three thermoplastic polymers, a mixture of polyvinyl alcohol containing 15–50 wt.% Of a mixture of water with glycerin is fed into an extruder connected to a co-electrocrusive head, the mixture is heated to 150–210 ° C under a pressure of 30–70 atm, reduce pressure to atmospheric, with simultaneous removal of released vapors before the mixture enters the co-extrusion head, thermoplastic polymer is separately fed at 120-200s, flow is connected at a temperature difference from 1 to 70 ° C and a speed difference from +10 to - 10% between flow m PVA and flow of the thermoplastic polymer and molded product. A mixture of polyvinyl alcohol contains 7–20 wt.% Water and 8–25 wt.% Glycerol. The temperature in the feed zones, compression, pressure drop, recompression, distribution zone and co-extrusion head is 140-200, 150-210, 170-220, 170-215, and 160-200 C, respectively. The method includes the following general steps: feeding a polyvinyl alcohol with a high degree of hydrolysis into an extruder connected to a coextrusion head, including a plasticizer-containing mixture of plasticizing compounds as water, and heated under pressure to a temperature at which it passes into a plastisol; the rapid drop in pressure of polyvinyl alcohol, which is in the state of plastisol, while simultaneously evaporating the released vapors before the specified polymer is introduced into the coextrusion head and while maintaining a temperature at least equal and predominantly higher than the co-extrusion temperature heads; Separate feeding into the same co-extrusion head of at least another thermoplastic polymer in the molten state; controlling the temperature of the polymers by contacting them with each other so that the temperature of the polyvinyl alcohol is at least equal to or higher than the temperature of the other co-molded polymer or polymers; regulation of the flow rate of polymers so that their linear output rates are equal or differ by a maximum of. The layered products obtained by the method described above consist of two or more joined together and jointly pressed layers of thermo plastic material in which at least one layer is made of polyvinyl alcohol, uniformly distributed over the entire surface of the specified product. The thickness of the polyvinyl alcohol layer can vary widely, typically from 100 microns to several millimeters. The thickness of the other layers depends on what the durability of the finished product requires, i.e. from the field of its use. The component that provides impermeability of the product to gases, vapors and odors is usually polyvinyl alcohol, while resistance to water and chemical reagents is attached to the product by another co-extruded polymer. As a consequence, the number, the order of the layers that are joined together and jointly pressed together and the type of thermoplastic polymer that is pressed through with polyvinyl alcohol depends on the intended use and on the desired properties of the products. I For example, for the manufacture of bottles or cylinders for carbonated beverages, the number of layers must be at least three, mainly of polyolefin, which is resistant to water and chemical reagents. In the manufacture of internal chambers for pressurized vessels, in which the product is kept under sterile conditions, and at least two layers are necessary to penetrate into the internal chamber of the gas present in the space between the internal chamber and the fixed vessel body. the inner one is polyolefinic and the outer one is polyvinyl alcohol. 1 A layer of polyvinyl alcohol may be internal in the case; when an anhydrous substance compatible with polyvinyl alcohol is in the vessel. Any polyvinyl alcohol with a polymerization degree of 1000-1100 and with a degree of hydrolysis of at least 85 mol.% Can be used. Polyvinyl alcohol with a degree of polymerization of more than 900 is most practically applicable, since a film having a sufficiently high mechanical strength is obtained from it. As a thermoplastic polymer using polyethylene, nylon b.
    nylon 66, polyethylene terephtelate, polyvinyl chloride.
    Most preferred are low density polyethylene (0.914-0.930), high density polyethylene (0.930-0.970),
    Conducted tests showed that IHTO co-pushes polyvinyl alcohol with at least one other thermoplastic polymer in order to obtain two-layer or multi-layer jointly extruded products, and mainly closed-surface products, possibly under conditions that provide good processing ability of the material, and under the conditions of forming a homogeneous layer of polyvinyl alcohol over the entire surface of the product, and specifically:
    increasing the temperature of the polyvinyl alcohol before the polymer is introduced into the co-extrusion head to the temperature of the polymer in the area of the co-extrusion head;
    removing vapors emitted by the polyvinyl alcohol at the above temperature and under pressure drop conditions;
    maintaining the temperature of the polyvinyl alcohol in the co-extrusion head equal to or higher than the temperature of the other jointly pressed polymer jointly forcing both melted polymers with the same linear velocity or velocity difference not exceeding -10%.
    In the practical implementation of the invention, the molten mass, especially the mass of polyvinyl alcohol, must be in a state of continuous movement, thus preventing any flow retardation both in the extruder and in the coextrusion head, and therefore the polyvinyl alcohol must have flowability and flow rate minimizing the back pressure needed to produce a homogeneous product at the outlet.
    In addition, during the transformation of a co-extruded tube into a processed product, especially into two-layer products, the formation of such a tube should occur as quickly as possible (not more than 5 minutes).
    The bilayer co-extruded tube exiting the coextrusion head is subjected to different treatments depending on the final destination. For example, in the case of making films, the parison, the film coming out of the co-extrusion head, is cooled from the outside and the air is blown into the socket at a pressure sufficient to support and stretch the material that has been jointly pressed.
    In the manufacture of containers, such as bottles, chambers, and so on, a co-extruded tube coming out of the co-extrusion head is clamped between the die section, and the pressurized air is blown into the inside of the tube section that is in the die. matrices, calibrate and cool the tube obtained in accordance with methods known in the art.
    Polyvinyl alcohol introduced with a water-containing mixture of plasticizers is transformed into a plastisol state by heating to a temperature of above 150 ° C in an extruder under pressure, which varies depending on the working conditions and the amount of plasticizer added, and is usually above 30 atm. .
    0
    The polyvinyl alcohol mass, after it is transferred to the plastisol state, is heated to the temperature of the co-extrusion head, quickly depressurises, and the gas is vented to release excess water vapor or other volatile components contained in the polymer under thermodynamic equilibrium.
    To accelerate the removal of vapors and to prevent their condensation.
    0, the vapors released in such a gas outlet are sucked by an exhaust fan.
    To supply polyvinyl alcohol to the coextrusion head, use
    5 extruders with a large length-to-diameter ratio, for example extruders with a length-to-diameter ratio of more than 25. In addition, the design of the coextrusion head should prevent
    0 possible mixing of plastic materials directed into it.
    The flow rate of polyvinyl alcohol is maintained predominantly constant, fast and uniform in order to eliminate both flow retardation and decomposition of the polymer.
    The temperature of the plastisol mass of polyvinyl alcohol is at least equal to and preferably higher than the temperature of the other co-extruded polymer or polymers in the process of contacting them with each other in the coextrusion head, and the temperature difference should not exceed 70 ° C.
    In order to impart sufficient fluidity to polyvinyl alcohol under conditions of melting, it is plasticized with a mixture of water with a multi-valent alcohol, taken in such quantity that their sum does not exceed 50 weight,% of the amount of polyvinyl alcohol, preferably 720 wt.% Water and 8- 25 wt.% Multivalent alcohol. As plasticizers of polyvinyl alcohol, for example, ethylene glycol, triethylene glycol, polyethylene glycol, glycerin, and trimeti-lenpropane are used. To impart a high heat resistance to polyvinyl alcohol, 1–3 parts by weight is added to it. stearate metachla per 100 weight parts, belonging to I or 1. group of elements of the periodic Periodic table. Composition based on polyvinyl alcohol, subjected to joint punching, if necessary, be introduced together with lubricants, pigments or other known irradiation. FIG. Figure 1 shows a co-extrusion device (co-pushing devices) consisting of two extruders connected to a coextrusion head, and in which a two-layer co-extruded tube (parison) enters an open matrix, a common figure in FIG. 2 the same in which one of the extruders simultaneously feeds the CC1 inner layer and the outermost layer of a three-layer jointly presented tube (parison), and in which this three layer on the tube (parison) is guided into an open matrix; in fig. 3 - the same consisting of three extruders connected to a co-extrusion head and in which a three-layer extruded tube (parison) is connected to a blowing device for tubular films; in fig. 4 - the same, in which one of the extruders simultaneously provides the inner and outer layers of a three-layer tube (parison), which is directed to a calibrating and cooling device; in fig. 5 is a vessel made on the proposed device (some parts have a three-dimensional image). Polyvinyl alcohol, introduced with water, a multivalent alcohol, lubricants and stabilizers, is fed into the extruder 1 through a feed hopper 2 and then into a co-extrusion head 3. A thermoplastic polymer, subjected to joint punching with polyvinyl alcohol, is fed into the same coextrusion head 3 through the extruder 4, which is equipped with a feed funnel 5.; The extruder 1 for polyvinyl alcohol has a large ratio. the length to the diameter, and the screw has a shape that divides the extruder into five zones, each From which it maintains s at a different regulated temperature, which rises until it reaches the maximum value in the third zone, corresponding to the pressure drop zone, Exeder 1 includes the following zones: - polymer supply zone A with a temperature of 140-200 ° Cj - zone B of compression, with a temperature of 150210 ° C, in which the plasticization of the polymer takes place, zone C of decompression (pressure drop) with a temperature of 17 ° C - 220 ° Cj; zone D of recompression with a temperature of 170-215 ° C; WITH. The extruder 1 is provided with a hole 6 located adjacent to the decompression zone through which, with a pressure drop, all the vapors separated by the plasticized polymer are removed. Vapor removal can be accelerated with an exhaust fan. Polyvinyl alcohol, in the state of plastisol and subjected to deaeration, is fed to a coextrusion head 3, in which the temperature is kept lower than in the C zone of decompression, preferably 160200 C. The thermoplastic polymer in a granular or powdery form, which quickly melts and plasticizes at heated to 120,200 s, supplied by an extruder 4. The temperature of this thermoplastic polymer must be lower than the temperature of one of the polyvinyl alcohols at the moment when both polymers contact each other. another in the coextrusion head. As shown in FIG. 1, both extruders 1 and 4 are connected to a co-extrusion head 3 having two concentrically arranged holes 7 and 8, the polyvinyl alcohol being forced through the outer hole 7 and the other polymer being forced through the inner hole 8. As shown in FIG. 2, two extruders 1 and 4 are connected to an extrusion head 3 having three concentric holes 9 and 10 and 11, the polyvinyl alcohol being forced through the central hole 10, and the other polymer through the external hole 9 and the internal hole 11. The device (FIG. 3) a co-extrusion head 3 is used, having three concentrically arranged openings 9,10 and 11 relating to different extruders. Thus, there are three such extruders, of which extruders feeding the product to the external opening 9 and to the internal opening 11 are similar to the extruder 4, while the extruder feeding the material to the intermediate opening 10 is similar to the extruder 1. The coextrusion head in FIG. 4 is similar to the head nafig. 2, but both extruders 1 and 4 are located along the extrusion axis. A jointly pressed tube (parison) 12, coming out of the coextrusion head 3, can be gripped between sections 13 and 14 of the matrix 15 and supported by conventional means under the coextrusion head 3 and is aligned with respect to the outlet of the specified head (Fig. 1.2) . In one embodiment, the extruded tube (parison) 12 may also be converted into a tubular film by blowing air into the socket 6 and by cooling the outside of the tubular film stretched by means of a cooling ring 7. In FIG. 4 shows the obtaining of tube 18 by calibration and simultaneous cooling of a jointly pressed tube (parison) 12 using a known device 19. The screw has such a shape that it divides the extruder into five zones: feed zone A, in which the thread height is maintained constant; Compression zone, in which the compression ratio is 3: 1; With the decompression zone, in which the decompression coefficient is 4: 1; the recompression zone D, in which the compression ratio is 2: 1; feed zone E, in which the thread height is kept constant. In each of the five zones, the following temperatures are created: zone A 190Cg zone B, zone C 205 ° C, zone D 200s, zone E 190s. Directly near zone C, a mixture of polymer and plasticizer is sucked through a hole located in the extruder jacket. Such absorption of the mixture can be accelerated by installing a vacuum-creating device at the top of the hole. Polyvinyl alcohol in the state of plastisol is fed through an extruder into the outer hole of the coextrusion head at. The inner bore of this coextrusion head is connected to another conventional extruder, through which the low density molten polyethylene passes through. A co-extruded tube exiting the coextrusion die passes between the two sections of the blown die and turns into a hollow vessel. The resulting hollow vessel weighing about 16 g has a volume of 110 cm, the thickness of the outer layer is about 400 microns, the inner one is 600 microns The thickness of the oxygen to oxygen, nitrogen. The carbon dioxide and fluorinated and chlorinated gases of the thus-obtained hollow vessel are practically zero at pressures from 1 atm to pressing force. Example 1. To 100 weight.h. polyvinyl alcohol with a degree of polymerization of about 1000 and with a degree of hydrolysis of 88-89 mol.%, 20 parts by weight are added. water, 20 weight.h. glycerol and 1 weight.h. zinc stearate. The mixture is fed into a screw extruder connected to a coextrusion head having two concentrically arranged holes and with a ratio of length to diameter 28. Example 2. to 100 weight parts. polyvinyl alcohol with a degree of polymerization of 1100 and with a degree of hydrolysis of 88-89 mol.%, 10 parts by weight are added. water and 10 weight.h. glycerol. The mixture is transformed into the plastisol state of Example 1 and, after deaeration, is directed to the middle hole of the co-extrusion head, in which the temperature is maintained at 170 ° C. The other two holes, internal and external, are connected to one extruder, through which low-density polyethylene is fed 140 C. Examples of the use of other thermoplastic polymers for co-extrusion with polyvinyl alcohol are given in the table.
    Polyvinyl chloride 155-160
    Polyethylene terephthalate190
    Nylon 6,66200
    0.045
    0.044 0.039
    In tested flasks, the thermoplastic polymer was used as the outer layer, and polyvinyl alcohol as the inner layer.
    权利要求:
    Claims (4)
    [1]
    1. A laminated product consisting of two or three alternating layers made of thermoplastic materials, characterized in that, in order to improve gas tightness, one layer is made of polyvinyl alcohol with a degree of polymerization of 1000-1100 and a degree of hydrolysis of 88-89 mol. %, and another layer is made of a thermoplastic polymer selected from the group including polyethylene, polyvinyl chloride, polyethylene tereft and nylon.
    [2]
    2. Method of making a layered product by co-extrusion of two or three thermoplastic polymers, it is necessary that a mixture of polyvinyl alcohol containing 15-50% by weight of water-glycerin mixture is heated to 15O in an extruder connected to a coextrusion head. -210 ° С. Under pressure of 30-70 atm, reduce pressure to atmospheric, s
    simultaneously removing the released vapors before the mixture reaches the co-extrusion head, a thermoplastic polymer is separately fed at 120–200 ° C, the flow is connected at a temperature difference from 1 to and a speed difference from +10 to –10% between the flow of polyvinyl alcohol and the flow thermoplastic polymer and molded product.
    [3]
    3. A process according to claim 2, characterized in that the mixture of polyvinyl alcohol is processed, containing 7-20% by weight of water and 8-25% by weight of glycerin.
    [4]
    4. Method according to paragraphs. 2 and 3, characterized in that the temperature in the delivery zones, compression, pressure drop, recompression, distribution zone and coextrusion go are 140200, 150-210, 170-220, 170-215, 170205 and 1bO-200, respectively.
    Sources of information taken into account in the examination
    1. US patent number 3900691,
    cl. In 32 B27 / 32, published. 1975.
    2. US patent number 3865665,
    cl. In 29 F 3/00, published. 1975.
    Fig 2.
    类似技术:
    公开号 | 公开日 | 专利标题
    SU871735A3|1981-10-07|Lamellar article and its manufacturing method
    US4112181A|1978-09-05|Method for preparing a film of vinylidene chloride polymer
    US3821182A|1974-06-28|Method for preparing of film of a vinylidene chloride polymer
    US4048428A|1977-09-13|Method for preparing a film of vinylidene chloride polymer
    US4379117A|1983-04-05|Method for preparing a film of vinylidene chloride polymer
    US4064296A|1977-12-20|Heat shrinkable multi-layer film of hydrolyzed ethylene vinyl acetate and a cross-linked olefin polymer
    EP0110493B1|1991-12-04|Method for producing a multi-layered plastics container
    US3337665A|1967-08-22|Method for the production of thermoplastic film
    CA1335223C|1995-04-11|Ethylene-vinyl alcohol copolymer composition and multilayered structure utilizing the same
    US4800129A|1989-01-24|Multi-layer plastic container
    US4512948A|1985-04-23|Method for making poly| article
    US4476170A|1984-10-09|Poly| articles and method
    US4436778A|1984-03-13|Multilayer tubular body with uncentered barrier layer
    KR960008301B1|1996-06-24|Biaxially oriented multilayer barrier films
    EP0076366B1|1987-09-02|Multilayer tubular body with uncentered barrier layer
    AU740936B2|2001-11-15|Biaxially oriented fluoropolymer films
    US4579784A|1986-04-01|Laminates on the basis of polypropylene and process for preparing such laminates
    DK143060C|1990-06-25|Plastic bottle for liquids under gas pressure and practically resistant to deformation caused by pressure and to the penetration of gases and liquids, as well as to its process
    US4294935A|1981-10-13|Method of producing ethylene-vinyl alcohol copolymer film
    US5788926A|1998-08-04|Plastic bottle and process for making the same
    NZ203100A|1986-06-11|Blow moulding then heat setting poly|articles
    USH469H|1988-05-03|Clear plastic container with good gas and water vapor barrier properties
    CA1277467C|1990-12-11|Method of manufacturing polybutylene terephthalate resin films
    US20050082713A1|2005-04-21|Method of making oriented polychlorotrifluoethylene films
    EP3287472B1|2021-09-29|Ethylene-vinyl alcohol copolymer, manufacturing method therefor, and laminate
    同族专利:
    公开号 | 公开日
    AT372903B|1983-11-25|
    NL7701534A|1977-08-22|
    GB1544780A|1979-04-25|
    AU511816B2|1980-09-04|
    DE2706882C2|1987-05-14|
    AU2237877A|1978-08-24|
    NL189238C|1993-02-16|
    CH616365A5|1980-03-31|
    DK154615B|1988-12-05|
    ATA102777A|1983-04-15|
    GR82304B|1984-12-13|
    SE428542B|1983-07-11|
    BR7701061A|1977-10-18|
    JPS52100561A|1977-08-23|
    IN145943B|1979-01-20|
    CS210611B2|1982-01-29|
    FR2341433A1|1977-09-16|
    ES456391A1|1978-01-16|
    YU42977A|1982-05-31|
    YU39184B|1984-08-31|
    NL189238B|1992-09-16|
    SE7701622L|1977-08-19|
    DK154615C|1989-05-22|
    FR2341433B1|1981-07-03|
    HU179544B|1982-11-29|
    DE2706882A1|1977-09-01|
    CA1090971A|1980-12-09|
    DK62377A|1977-08-19|
    JPS6140536B2|1986-09-10|
    US4244914A|1981-01-13|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    RU2447995C2|2011-03-09|2012-04-20|Алексей Николаевич Докукин|Method of extruding flat thread from synthetic raw stock|
    RU2448831C2|2011-03-09|2012-04-27|Алексей Николаевич Докукин|Extrusion line for producing flat thread from synthetic raw stock|GB1026349A|1961-10-27|1966-04-20|Kurashiki Rayon Kk|Method of manufacturing thin films of polyvinyl alcohols|
    US3365413A|1963-07-23|1968-01-23|Monsanto Co|Polyvinyl alcohol films plasticized with monophenyl ether of polyoxyethylene|
    US3440316A|1963-12-05|1969-04-22|Kuraray Co|Method of manufacturing improved polyvinyl alcohol films|
    US3561493A|1965-04-21|1971-02-09|Paul Maillard|Composite tubes and method of manufacturing same|
    US3607812A|1968-12-17|1971-09-21|Denki Kagaku Kogyo Kk|Method of manufacturing polyvinyl alcohol films and product|
    DE1965856A1|1968-12-24|1970-09-10|Kurashiki Spinning Co Ltd|Packaging containers and processes for their manufacture|
    US3679437A|1969-05-26|1972-07-25|Tee Pak Inc|Preparation of fibrous reinforced sausage-type casings from melt-extruded polyvinyl alcohol resins|
    JPS5141157B2|1972-08-08|1976-11-08|
    DE2345049A1|1973-09-06|1975-03-20|Breyer Anton Fa|Thermoplastic laminates from plastics of differing props. - by heating different plastics in separate thermally insulated channels|
    JPS5223368B2|1973-11-26|1977-06-23|GB1579872A|1977-03-08|1980-11-26|Ucb Sa|Cylindrical container body for packaging pressurised and nonpressurised materials|
    FR2416784B1|1978-02-13|1981-05-29|Rhone Poulenc Ind|
    DE3071454D1|1979-11-28|1986-04-03|Wirsbo Bruks Ab|GASEOUS DIFFUSION RESISTANT ARTICLE|
    DE3047181A1|1980-12-15|1982-06-16|Hoechst Ag, 6000 Frankfurt|PLASTIC PIPE WITH OXYGEN-COATING|
    FR2507125B1|1981-06-03|1984-01-13|Rhone Poulenc Spec Chim|
    US4731266A|1981-06-03|1988-03-15|Rhone-Poulenc, S.A.|Water-resistant polyvinyl alcohol film and its application to the preparation of gas-impermeable composite articles|
    JPH0231661B2|1981-11-28|1990-07-16|Basf Ag|
    US4536532A|1982-05-27|1985-08-20|Miller Gerald W|Plasticized polyvinyl alcohol compositions, forming process and formed articles|
    US4478971A|1983-07-08|1984-10-23|Shakespeare Company|High temperature extruded polyvinyl alcohol monofilament and process for the preparation thereof|
    US4649004A|1983-12-27|1987-03-10|Toyo Seikan Kaisha, Ltd.|Process for production of multi-layer pipes for draw-forming|
    EP0179093A4|1984-04-12|1987-10-08|Baxter Travenol Lab|Container such as a nursing container, with flexible liner and access site and method of making same.|
    US4558792A|1984-04-12|1985-12-17|Baxter Travenol Laboratories, Inc.|Container such as a nursing container, with flexible liner and access site and method of making said access site|
    GB2163386A|1984-07-20|1986-02-26|Windmoeller & Hoelscher|Co-extruding a substrate web of synthetic thermoplastic material and an adhesive layer consisting of a non-crosslinkable elastomer|
    DE3510395C2|1985-03-22|1987-11-05|Technoform Caprano + Brunnhofer Kg, 3501 Fuldabrueck, De|
    US4942008A|1985-07-10|1990-07-17|Cahill John W|Process for molding a multiple layer structure|
    US4643927A|1985-07-18|1987-02-17|The Dow Chemical Company|Tubular, multi-layer film and method of making|
    CA1296852C|1985-10-11|1992-03-10|Henry George Schirmer|High oxygen barrier coextruded film|
    JPH0358567B2|1986-03-31|1991-09-05|Toyo Seikan Kaisha Ltd|
    GB8630863D0|1986-12-24|1987-02-04|Grace W R & Co|Laminated articles|
    DE3700237A1|1987-01-07|1988-07-21|Bekum Maschf Gmbh|CO EXTRUSION HEAD|
    US4822547A|1987-04-06|1989-04-18|Shell Oil Company|Process for the extrusion of compositions comprising polypropylene, polyvinyl alcohol and a polypropylene-polyvinyl alcohol adhesive|
    US4906421A|1987-07-01|1990-03-06|Avery International Corporation|Process for making high performance pressure sensitive adhesive tapes|
    SE8704657L|1987-11-24|1989-05-25|Plm Ab|BEHAALLARE|
    US4851168A|1988-12-28|1989-07-25|Dow Corning Corporation|Novel polyvinyl alcohol compositions and products prepared therefrom|
    US5051222A|1989-09-01|1991-09-24|Air Products And Chemicals, Inc.|Method for making extrudable polyvinyl alcohol compositions|
    US5137969A|1989-09-01|1992-08-11|Air Products And Chemicals, Inc.|Melt extrudable polyvinyl alcohol pellets having reduced maximum melt temperature and reduced gel content|
    DE69002295T2|1989-09-25|1993-11-04|Schneider Usa Inc|MULTILAYER EXTRUSION AS A METHOD FOR PRODUCING BALLOONS FOR VESSEL PLASTICS.|
    DE4001126C1|1989-11-20|1990-12-13|Technoform Caprano + Brunnhofer Kg, 3501 Fuldabrueck, De|
    FR2662638B1|1990-05-31|1997-09-05|Nok Corp|COLD RESISTANT LAMINATED SHEET GAS BARRIER, BLADDER FOR ACCUMULATOR AND ACCUMULATOR COMPRISING SAME.|
    US5798152A|1990-07-24|1998-08-25|Novon International|Biodegradable composite polymeric articles comprising polyvinyl alcohol|
    US5195969A|1991-04-26|1993-03-23|Boston Scientific Corporation|Co-extruded medical balloons and catheter using such balloons|
    CA2116679C|1991-10-01|2003-11-04|David B. Herridge|Coextruded pressure-sensitive adhesive tape and method of making|
    US5589122A|1991-10-01|1996-12-31|Minnesota Mining And Manufacturing Company|Method of making double-sided pressure-sensitive adhesive tape|
    US5520223A|1994-05-02|1996-05-28|Itt Industries, Inc.|Extruded multiple plastic layer coating bonded to the outer surface of a metal tube having an optical non-reactive inner layer and process for making the same|
    US6321795B1|1992-04-14|2001-11-27|Itt Industries, Inc.|Multi-layer fuel and vapor tube|
    US5678611A|1992-04-14|1997-10-21|Itt Corporation|Multi-layer fuel and vapor tube|
    US5884672A|1992-04-14|1999-03-23|Itt Industries, Inc.|Multi-layer fuel and vapor tube|
    US6378562B1|1992-04-14|2002-04-30|Itt Industries, Inc.|Multi-layer tubing having electrostatic dissipation for handling hydrocarbon fluids|
    US5524673A|1992-04-14|1996-06-11|Itt Corporation|Multi-layer tubing having electrostatic dissipation for handling hydrocarbon fluids|
    US5865218A|1992-04-14|1999-02-02|Itt Corporation|Multi-layer fuel and vapor tube|
    AU4021493A|1992-04-23|1993-11-29|British Technology Group Inter-Corporate Licensing Limited|Polymeric articles and materials|
    WO1995009667A1|1993-10-01|1995-04-13|Boston Scientific Corporation|Medical device balloons containing thermoplastic elastomers|
    US6896842B1|1993-10-01|2005-05-24|Boston Scientific Corporation|Medical device balloons containing thermoplastic elastomers|
    US5590691A|1994-05-02|1997-01-07|Itt Corporation|Extruded multiple plastic layer coating bonded to a metal tube|
    US5566720A|1995-01-10|1996-10-22|Itt Corporation|Elongated fuel and vapor tube having multiple layers and method of making the same|
    US6130404A|1997-03-03|2000-10-10|Itt Automotive, Inc.|Electro-optical removal of plastic layer bonded to a metal tube|
    US6180197B1|1998-02-13|2001-01-30|Itt Manufacturing Enterprises, Inc.|Multi-layer tubing having at least one intermediate layer formed from a polyamide/polyketone alloy|
    US6257281B1|1998-02-13|2001-07-10|Itt Manufacturing Enterprises, Inc.|Multi-layer tubing having at least one intermediate layer formed from a polyamide alloy|
    SE511766C2†|1998-03-23|1999-11-22|Wirsbo Bruks Ab|Plastic multilayer tubes and their use|
    AU3172799A|1998-04-20|1999-11-08|Kwang Myung Pharm. Ind. Co., Ltd.|Compositions of polyolefin and polyvinyl alcohol, and films, sheets and articlesprocessed therefrom and multilayer products using the same|
    US5960977A|1998-05-14|1999-10-05|Itt Manufacturing Enterprises, Inc.|Corrugated polymeric filler neck tubing|
    US6240970B1|1999-04-01|2001-06-05|Itt Manufacturing Enterprises, Inc.|Tubing for handling hydrocarbon materials and having an outer jacket layer adhered thereto|
    US6276400B1|1999-06-08|2001-08-21|Itt Manufacturing Enterprises, Inc.|Corrosion resistant powder coated metal tube and process for making the same|
    US7947059B2|2000-03-02|2011-05-24|Boston Scientific Scimed, Inc.|Multilayer medical device|
    GB2366781A|2000-09-19|2002-03-20|Shya Hsin Plastic Works Co Ltd|Three-layer moulded container|
    CN1209425C|2001-07-04|2005-07-06|三菱丽阳株式会社|Plastic sol composition, gel film and product|
    US7488339B2|2002-10-21|2009-02-10|Boston Scientific Scimed, Inc.|Multilayer medical device|
    US6951675B2|2003-01-27|2005-10-04|Scimed Life Systems, Inc.|Multilayer balloon catheter|
    DE10347907A1|2003-10-15|2005-05-25|Bernd Hansen|Method and device for producing filled and closed containers|
    DE102004004755A1|2004-01-30|2005-08-25|Bernd Hansen|Method and device for producing and filling containers|
    CA2711750A1|2007-10-29|2009-05-07|Belmay, Inc.|Bio-plastic composite material, method of making same, and method of using same|
    US9221204B2|2013-03-14|2015-12-29|Kortec, Inc.|Techniques to mold parts with injection-formed aperture in gate area|
    CN111319211B|2020-03-11|2021-05-04|苏州喜全软件科技有限公司|Continuous forming printing device for plastic extrusion pipe fitting|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    IT2028176A|IT1055976B|1976-02-18|1976-02-18|Multilayer thermoplastic sheets prepd. by coextrusion - of polyvinyl alcohol plastisol and pref. polyolefin partic. for blow moulding applications|
    IT2028076A|IT1055900B|1976-02-18|1976-02-18|Multilayer thermoplastic sheets prepd. by coextrusion - of polyvinyl alcohol plastisol and pref. polyolefin partic. for blow moulding applications|
    [返回顶部]